Canonical Allele Identifier: PA1139749771
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 834611
ClinVar RCV Id: RCV001035334 RCV002258087 RCV004004690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Trp45Gly
CA379966317
NM_024426.6:c.133T>G